Canonical Allele Identifier: CA1979584248
Community Standard Title: NM_018026.4(PACS1):c.661-15T>A
Gene: PACS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66216104T>A , CM000673.2:g.66216104T>A GRCh38
NC_000011.9:g.65983575T>A , CM000673.1:g.65983575T>A GRCh37
NC_000011.8:g.65740151T>A NCBI36
NG_033900.1:g.150752T>A

Transcript Alleles

HGVS Amino-acid Change
NM_018026.4:c.661-15T>A MANE Select NP_060496.2:n.661-15T>A
ENST00000320580.9:c.661-15T>A MANE Select ENSP00000316454.4:n.661-15T>A
NM_018026.3:c.661-15T>A NP_060496.2:n.661-15T>A
ENST00000320580.8:c.661-15T>A ENSP00000316454.4:n.661-15T>A
ENST00000527224.1:n.785-15T>A
ENST00000527380.1:c.367-15T>A ENSP00000432639.1:n.367-15T>A
XM_011545162.1:c.340-15T>A XP_011543464.1:n.340-15T>A
XM_011545163.1:c.331-15T>A XP_011543465.1:n.331-15T>A
XM_011545164.1:c.322-15T>A XP_011543466.1:n.322-15T>A
XM_011545164.2:c.322-15T>A XP_011543466.1:n.322-15T>A
XR_001747924.1:n.872-15T>A